US3168588A - Polymerized ethylene lubricating oils from alkanol modified catalysts - Google Patents

Polymerized ethylene lubricating oils from alkanol modified catalysts Download PDF

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US3168588A
US3168588A US55845A US5584560A US3168588A US 3168588 A US3168588 A US 3168588A US 55845 A US55845 A US 55845A US 5584560 A US5584560 A US 5584560A US 3168588 A US3168588 A US 3168588A
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alkanol
catalyst
ethylene
aluminum
transition metal
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Herschel T White
Jr Arthur W Langer
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ExxonMobil Technology and Engineering Co
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Exxon Research and Engineering Co
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Priority to GB30054/61A priority patent/GB920145A/en
Priority to US413347A priority patent/US3474157A/en
Publication of US3168588A publication Critical patent/US3168588A/en
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Priority to US783699A priority patent/US3662021A/en
Priority to US05/882,946 priority patent/US4396788A/en
Priority to US06/179,655 priority patent/US4409414A/en
Priority to US06/330,596 priority patent/US4442309A/en
Anticipated expiration legal-status Critical
Priority to US06/454,379 priority patent/US4486615A/en
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    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J31/00—Catalysts comprising hydrides, coordination complexes or organic compounds
    • B01J31/02—Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides
    • B01J31/12—Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides containing organo-metallic compounds or metal hydrides
    • B01J31/14—Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides containing organo-metallic compounds or metal hydrides of aluminium or boron
    • B01J31/143—Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides containing organo-metallic compounds or metal hydrides of aluminium or boron of aluminium
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J31/00—Catalysts comprising hydrides, coordination complexes or organic compounds
    • B01J31/02—Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides
    • B01J31/0201—Oxygen-containing compounds
    • B01J31/0202—Alcohols or phenols
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J31/00—Catalysts comprising hydrides, coordination complexes or organic compounds
    • B01J31/26—Catalysts comprising hydrides, coordination complexes or organic compounds containing in addition, inorganic metal compounds not provided for in groups B01J31/02 - B01J31/24
    • B01J31/36—Catalysts comprising hydrides, coordination complexes or organic compounds containing in addition, inorganic metal compounds not provided for in groups B01J31/02 - B01J31/24 of vanadium, niobium or tantalum
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J31/00—Catalysts comprising hydrides, coordination complexes or organic compounds
    • B01J31/26—Catalysts comprising hydrides, coordination complexes or organic compounds containing in addition, inorganic metal compounds not provided for in groups B01J31/02 - B01J31/24
    • B01J31/38—Catalysts comprising hydrides, coordination complexes or organic compounds containing in addition, inorganic metal compounds not provided for in groups B01J31/02 - B01J31/24 of titanium, zirconium or hafnium
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2/00—Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms
    • C07C2/02—Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms by addition between unsaturated hydrocarbons
    • C07C2/04—Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms by addition between unsaturated hydrocarbons by oligomerisation of well-defined unsaturated hydrocarbons without ring formation
    • C07C2/06—Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms by addition between unsaturated hydrocarbons by oligomerisation of well-defined unsaturated hydrocarbons without ring formation of alkenes, i.e. acyclic hydrocarbons having only one carbon-to-carbon double bond
    • C07C2/08—Catalytic processes
    • C07C2/26—Catalytic processes with hydrides or organic compounds
    • C07C2/30—Catalytic processes with hydrides or organic compounds containing metal-to-carbon bond; Metal hydrides
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F10/00—Homopolymers and copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10L—FUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
    • C10L1/00—Liquid carbonaceous fuels
    • C10L1/10—Liquid carbonaceous fuels containing additives
    • C10L1/14—Organic compounds
    • C10L1/16—Hydrocarbons
    • C10L1/1625—Hydrocarbons macromolecular compounds
    • C10L1/1633—Hydrocarbons macromolecular compounds homo- or copolymers obtained by reactions only involving carbon-to carbon unsaturated bonds
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2231/00—Catalytic reactions performed with catalysts classified in B01J31/00
    • B01J2231/10—Polymerisation reactions involving at least dual use catalysts, e.g. for both oligomerisation and polymerisation
    • B01J2231/12—Olefin polymerisation or copolymerisation
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2231/00—Catalytic reactions performed with catalysts classified in B01J31/00
    • B01J2231/20—Olefin oligomerisation or telomerisation
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J27/00—Catalysts comprising the elements or compounds of halogens, sulfur, selenium, tellurium, phosphorus or nitrogen; Catalysts comprising carbon compounds
    • B01J27/06—Halogens; Compounds thereof
    • B01J27/08—Halides
    • B01J27/10—Chlorides
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2527/00—Catalysts comprising the elements or compounds of halogens, sulfur, selenium, tellurium, phosphorus or nitrogen; Catalysts comprising carbon compounds
    • C07C2527/06—Halogens; Compounds thereof
    • C07C2527/133—Compounds comprising a halogen and vanadium, niobium, tantalium, antimonium or bismuth
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2527/00—Catalysts comprising the elements or compounds of halogens, sulfur, selenium, tellurium, phosphorus or nitrogen; Catalysts comprising carbon compounds
    • C07C2527/06—Halogens; Compounds thereof
    • C07C2527/135—Compounds comprising a halogen and titanum, zirconium, hafnium, germanium, tin or lead
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2531/00—Catalysts comprising hydrides, coordination complexes or organic compounds
    • C07C2531/02—Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides
    • C07C2531/12—Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides containing organo-metallic compounds or metal hydrides
    • C07C2531/14—Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides containing organo-metallic compounds or metal hydrides of aluminium or boron
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2531/00—Catalysts comprising hydrides, coordination complexes or organic compounds
    • C07C2531/26—Catalysts comprising hydrides, coordination complexes or organic compounds containing in addition, inorganic metal compounds not provided for in groups C07C2531/02 - C07C2531/24
    • C07C2531/36—Catalysts comprising hydrides, coordination complexes or organic compounds containing in addition, inorganic metal compounds not provided for in groups C07C2531/02 - C07C2531/24 of vanadium, niobium or tantalum
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2531/00—Catalysts comprising hydrides, coordination complexes or organic compounds
    • C07C2531/26—Catalysts comprising hydrides, coordination complexes or organic compounds containing in addition, inorganic metal compounds not provided for in groups C07C2531/02 - C07C2531/24
    • C07C2531/38—Catalysts comprising hydrides, coordination complexes or organic compounds containing in addition, inorganic metal compounds not provided for in groups C07C2531/02 - C07C2531/24 of titanium, zirconium or hafnium
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S585/00—Chemistry of hydrocarbon compounds
    • Y10S585/929—Special chemical considerations
    • Y10S585/946—Product is waxy polymer

Definitions

  • This invention relates to an improved method of preparing hydrocarbon oils. More particularly, it relates to polymerizing ethylene-containing gases to obtain oils having a molecular weight of about 802,000.
  • hydrocarbon oils having a minimum viscosity index of 140 and a molecular weight in the range of 350 to 800 could be prepared by polymerizing ethylene with controlled catalysts, diluents and under controlled temperatures.
  • the catalyst consisted of a transition metal halide and a halogenated aluminum alkyl compound.
  • the lower alkanols utilized are those in the C to C range, preferably C to C
  • the improvement from the use of the alkanol increases with molecular weight within the stated range. It has also been found that the structure of the alkanol is important.
  • the yield increased markedly upon changing from primary to secondary to tertiary alcohol.
  • the selectivity to polymer oil was considerably higher for secondary butanol and tertiary butanol than for isobutanol.
  • the alkanols that can be used include methanol, ethanol, n-propanol, isopropanol, n butanol, sec-butanol, tertiary butanol, isobutanol and all of the C and C alcohols.
  • C to C diols in which the hydroxy groups are not attached to adjacent carbon atoms are also useful.
  • These alkanols are utilized in a minor amount, i.e., so that the ratio of ROH/ R (based on aluminum alkyl) after reduction of the transition metal is not greater than 0.5 (preferably 0.2 to 0.33).
  • the unmodified catalysts are solid, insoluble, reaction products obtained by partially reducing a reducible, heavy,
  • Preferred transition metal halides include chloride materials such as TiOl ZrCl VCl etc. It is also possible to start with a reduced heavy, transition metal halide such as TiCl
  • the formula of halogenated aluminum alkyl compound has been presented above. The n can represent average values since a mixture of aluminum diethyl chloride and aluminum ethyl dichloride is preferred in many instances.
  • halogenated derivatives be employed as contrasted to the hydrocarbon aluminum derivatives such as aluminum triethyl, aluminum triisobutyl, etc.
  • the amount of solid polymer increases as the value of n goes from 1 to 2.
  • An especially effective compound for use is aluminum ethyl dichloride.
  • the molar ratio atent C ice of aluminum compound to transition metal halide compound can be in the range of 0.1 to 20, preferably 2 to 5.
  • the initial concentrations of catalyst components are normally in the range of 0.0005411 mole per liter of diluent.
  • the alkanol can be added either to the transition metal halide or the aluminum alkyl halide prior to the addition of the other component. It is preferred to add it, however, to the aluminum alkyl halide.
  • Ethylene is unique in the instant invention in that other olefins do not respond to give similar products.
  • the lower olefins can be copolymerized with ethylene to a limited extent. For example, at high ratios of comonomer to ethylene, a maximum of about propylene can be incorporated into the copolymer. Butene-l and higher alpha olefins copolymerized to a much lesser extent as thesize of the olefin increases. Because of the high selectivity of this catalyst system for ethylene polymerization, a wide variety of ethylene-containing gases may be used as feeds.
  • feed mixtures containing a major proportion of a higher alpha olefin are operable in many cases, although catalyst activity and efficiency are highest when ethylene is the major component.
  • catalyst activity and efficiency are highest when ethylene is the major component.
  • the viscosity index of the products is adversely affected by excess branching so that the amount of higher olefin which enters the product should be controlled by limiting its concentration in the feed and/or adjusting the catalyst composition and polymerization conditions.
  • the process temperatures employed are below 70 C. and preferably a temperature of 10 to C. is utilized.
  • the reaction is carried out by first mixing in the proper proportions solutions of the catalyst components in the halogenated aromatic diluent, preferably C H Cl or C H Cl at temperatures 25 C. and in the absence of moisture, oxygen, and sulfur impurities.
  • the result ing alkanol modified, Ti halide/Al ⁇ alkyl halide/diluent coordination complex is believed to constitute the active polymerization catalyst.
  • the reaction pressure utilized is generally in the range of 0 to 50 p.s.i.g.
  • the selectivity to liquid product drops off sharply above the maximum temperature which depends upon the catalyst acidity, diluent polarity and the alcohol type.
  • the polymerization must be carried out in the presence of a halogenated aromatic hydrocarbon diluent preferably a dichlorobenzene or monochlorobenzene.
  • a halogenated aromatic hydrocarbon diluent preferably a dichlorobenzene or monochlorobenzene.
  • the use of aliphatic chlorinated solvents results in rapid catalyst deactivation, much lower 'efiiciencies and excessive branching.
  • the halogenated aromatic hydrocarbons can be used alone or in conjunction with other diluents such as heptane, benzene, xylene, etc., provided that the halogenated aromatic material comprises a minimum of 40 vol. percent of the total diluent mixture and the halogen ch? replaces at least one of the hydrogens of the aromatic ring.
  • the oils of this invention have a minimum boiling point of about 62 C.
  • the lube oil fraction has a minimum viscosity index of 140 and a molecular weight in the range of 350 to 800.
  • the lower boiling olefin products are valuable chemical raw materials, and the higher boiling, oil-soluble, semi-solids are active middle distillate pour point depressants.
  • Example 1 0.006 mole of TiCl and 0.012 mole of methanol in 300 ml. of monochlorobenzene were saturated with C H between and ()5 C. There was little or no reaction evident between the TiCL, and alcohol at this temperature for the minute period that alkyl aluminum halide Was absent from the system. 0.024 mole of Et AlCl in 400 ml. of chlorobenzene was introduced at ()5 C. The reactor temperature was increased to 15 C. and ethylene polymerization was continued for 2 hours. Out of 125 gms. of total product, 38 gms., Wt. percent, of 405 C.+distillation bottoms were obtained. This material blended 0.1 wt. percent in heating oil reduced the pour point from -17 to C.
  • This example demonstrates improved selectivity over unmodified catalysts to soluble wax which is an effective pour depressant.
  • Example 2 A test was run on the polymerization of ethylene in the presence and absence of minor amounts of isopropanol.
  • the catalyst comprised 0.006 mole TiCl 0.006 mole Et AlCl, and 0.024 mole EtAlCl in 1,000 ml. monochlorobenzene diluent. Titanium was reduced for 1 hour at 25 C. with 0.006 mole Et AlCl and 0.012 mole EtAlCl before addition of remaining components. Ethylene polymerization period was 2 hours at 25 C. The results are tabulated below.
  • Example 3 Tests were run on the polymerization of ethylene with various hydroxy-containing materials.
  • the catalyst comprised 0.006 mole TiCl 0.006 mole Et AlCl, 0.012 mole EtAlCl and 0.006 mole of modifier in 1,000 rnl. monochlorobenzene diluent.
  • TiCl was reduced for 1 hour at 25 C. with the mixed alkyl aluminum halide before the modifier was added.
  • Ethylene was polymerized for 2 hours at 25 C. The results are tabulated below.
  • Example 5 A similar run is performed as in Example 3 but a temperature of C. and o-dichlorobenzene are used. Over 95% selectivity to oils is thus obtained. In general the more polar diiuents permit employment of higher temperatures Without producing solid polymers.
  • the products of this invention are useful as motor lube base stocks, olefinic synthetic intermediates, hydraulic transmission fluids, pour depressants, synthetic jet engine oils and bright stocks, among others. These products can also be hydrogenated without any diminution in viscosity index.
  • a method of preparing a hydrocarbon oil having a molecular weight in the range of 80 to 2000, said oil being suitable for lubricating purposes which comprises polymerizing an ethylene-containing gas in the presence of a catalyst consisting of a halide of a transition metal selected from the group consisting of titanium, zirconium, and vanadium and an aluminum alkyl compound having the formula AlR X n representing a number of at least 1.
  • the improvement which comprises utilizing a minor amount of a C -C alkanol as a catalyst modifier, said alkanol being present in an amount such that the ratio of alkanol to the alkyl of the aluminum alkyl after reduction of the transition metal halide is not greater than 0.5 1.
  • TiCl and the aluminum alkyl is aluminum ethyl dichloride.

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Description

United States This invention relates to an improved method of preparing hydrocarbon oils. More particularly, it relates to polymerizing ethylene-containing gases to obtain oils having a molecular weight of about 802,000.
It has been developed that hydrocarbon oils having a minimum viscosity index of 140 and a molecular weight in the range of 350 to 800 could be prepared by polymerizing ethylene with controlled catalysts, diluents and under controlled temperatures. The catalyst consisted of a transition metal halide and a halogenated aluminum alkyl compound.
It has now been found that increased oil yields and catalyst reactivity are obtained in the products desired by the utilization of a minor amount of a lower alkanol as a catalyst modifier. Additionally, improved molecular weight control is obtained.
It is surprising that the alkanols improve the process in that the presence of these materials is normally considered inconsistent with satisfactory catalyst performance in the systems used. In fact, the usual technique for inactivating catalyst at the end of a run is addition of excess alkanol (on catalyst).
The lower alkanols utilized are those in the C to C range, preferably C to C The improvement from the use of the alkanol increases with molecular weight within the stated range. It has also been found that the structure of the alkanol is important. For the butanol series (see table in Example 3), the yield increased markedly upon changing from primary to secondary to tertiary alcohol. Also, the selectivity to polymer oil (lower average molecular weight) was considerably higher for secondary butanol and tertiary butanol than for isobutanol. Thus, the alkanols that can be used include methanol, ethanol, n-propanol, isopropanol, n butanol, sec-butanol, tertiary butanol, isobutanol and all of the C and C alcohols. C to C diols in which the hydroxy groups are not attached to adjacent carbon atoms are also useful. Especially preferred and desirable are: tertiary butanol, secondary butanol, isoor n-butanol, and isopropanol. These alkanols are utilized in a minor amount, i.e., so that the ratio of ROH/ R (based on aluminum alkyl) after reduction of the transition metal is not greater than 0.5 (preferably 0.2 to 0.33). V
The unmodified catalysts are solid, insoluble, reaction products obtained by partially reducing a reducible, heavy,
transition metal halide of a Group IVB to VIB or VIII metal with a halogenated aluminum alkyl compound having the formula: AlR X n representing a number of at least 1 but less than 2. Preferred transition metal halides include chloride materials such as TiOl ZrCl VCl etc. It is also possible to start with a reduced heavy, transition metal halide such as TiCl The formula of halogenated aluminum alkyl compound has been presented above. The n can represent average values since a mixture of aluminum diethyl chloride and aluminum ethyl dichloride is preferred in many instances. It is essential that these halogenated derivatives be employed as contrasted to the hydrocarbon aluminum derivatives such as aluminum triethyl, aluminum triisobutyl, etc. The amount of solid polymer increases as the value of n goes from 1 to 2. An especially effective compound for use is aluminum ethyl dichloride. The molar ratio atent C ice of aluminum compound to transition metal halide compound can be in the range of 0.1 to 20, preferably 2 to 5. The initial concentrations of catalyst components are normally in the range of 0.0005411 mole per liter of diluent.
The use of these halogenated aluminum derivatives appears to be important for another reason. These compounds apparently control the amount of branching intro duced into the polymer product so as to obtain those having branching configurations consistent with the required viscosity indices. Thus non-halogenated aluminum derivatives result in the production of linear solid materials. Conversely, excessive Lewis acidity results in excessive branching and isomerization so that the desired products are not obtained.
The alkanol can be added either to the transition metal halide or the aluminum alkyl halide prior to the addition of the other component. It is preferred to add it, however, to the aluminum alkyl halide.
Ethylene is unique in the instant invention in that other olefins do not respond to give similar products. Although higher alpha olefins do not homopolymerize with the catalysts and conditions of this invention, the lower olefins can be copolymerized with ethylene to a limited extent. For example, at high ratios of comonomer to ethylene, a maximum of about propylene can be incorporated into the copolymer. Butene-l and higher alpha olefins copolymerized to a much lesser extent as thesize of the olefin increases. Because of the high selectivity of this catalyst system for ethylene polymerization, a wide variety of ethylene-containing gases may be used as feeds. Thus, feed mixtures containing a major proportion of a higher alpha olefin are operable in many cases, although catalyst activity and efficiency are highest when ethylene is the major component. Most important in this regard is the fact that the viscosity index of the products is adversely affected by excess branching so that the amount of higher olefin which enters the product should be controlled by limiting its concentration in the feed and/or adjusting the catalyst composition and polymerization conditions.
The process temperatures employed are below 70 C. and preferably a temperature of 10 to C. is utilized. The reaction is carried out by first mixing in the proper proportions solutions of the catalyst components in the halogenated aromatic diluent, preferably C H Cl or C H Cl at temperatures 25 C. and in the absence of moisture, oxygen, and sulfur impurities. The result ing alkanol modified, Ti halide/Al \alkyl halide/diluent coordination complex is believed to constitute the active polymerization catalyst. The reaction pressure utilized is generally in the range of 0 to 50 p.s.i.g. The selectivity to liquid product drops off sharply above the maximum temperature which depends upon the catalyst acidity, diluent polarity and the alcohol type. If o-dichlorobenzene (commercial grade) is substituted for monochlorobenzene, however, selectivity to oil 90% can be obtained in a tbutanol modified system at temperatures as high as C. Lower maximum polymerization temperatures must be used with less polar diluents and less branched alcohols.
The polymerization must be carried out in the presence of a halogenated aromatic hydrocarbon diluent preferably a dichlorobenzene or monochlorobenzene. The use of aliphatic chlorinated solvents results in rapid catalyst deactivation, much lower 'efiiciencies and excessive branching. The halogenated aromatic hydrocarbons can be used alone or in conjunction with other diluents such as heptane, benzene, xylene, etc., provided that the halogenated aromatic material comprises a minimum of 40 vol. percent of the total diluent mixture and the halogen ch? replaces at least one of the hydrogens of the aromatic ring.
The oils of this invention have a minimum boiling point of about 62 C. The lube oil fraction has a minimum viscosity index of 140 and a molecular weight in the range of 350 to 800. The lower boiling olefin products are valuable chemical raw materials, and the higher boiling, oil-soluble, semi-solids are active middle distillate pour point depressants.
This invention and its advantages will be better understood by reference to the following examples.
Example 1 0.006 mole of TiCl and 0.012 mole of methanol in 300 ml. of monochlorobenzene were saturated with C H between and ()5 C. There was little or no reaction evident between the TiCL, and alcohol at this temperature for the minute period that alkyl aluminum halide Was absent from the system. 0.024 mole of Et AlCl in 400 ml. of chlorobenzene was introduced at ()5 C. The reactor temperature was increased to 15 C. and ethylene polymerization was continued for 2 hours. Out of 125 gms. of total product, 38 gms., Wt. percent, of 405 C.+distillation bottoms were obtained. This material blended 0.1 wt. percent in heating oil reduced the pour point from -17 to C.
This example demonstrates improved selectivity over unmodified catalysts to soluble wax which is an effective pour depressant.
Example 2 A test was run on the polymerization of ethylene in the presence and absence of minor amounts of isopropanol. The catalyst comprised 0.006 mole TiCl 0.006 mole Et AlCl, and 0.024 mole EtAlCl in 1,000 ml. monochlorobenzene diluent. Titanium was reduced for 1 hour at 25 C. with 0.006 mole Et AlCl and 0.012 mole EtAlCl before addition of remaining components. Ethylene polymerization period was 2 hours at 25 C. The results are tabulated below.
Modifier, moles Isopro- None.
panel.
Yield, ml 330 300 Solid polymer:
M.W. l0- 14. 0 18. 6
Vol. percent 16 024-150 oil and soluble wax, vol percent 46 04- 4 olefins, vol. percent 45 34 This example demonstrates the increased activity and reduced mol. weight of the products obtained by the modified catalyst of this invention.
Example 3 Tests were run on the polymerization of ethylene with various hydroxy-containing materials. The catalyst comprised 0.006 mole TiCl 0.006 mole Et AlCl, 0.012 mole EtAlCl and 0.006 mole of modifier in 1,000 rnl. monochlorobenzene diluent. TiCl was reduced for 1 hour at 25 C. with the mixed alkyl aluminum halide before the modifier was added. Ethylene was polymerized for 2 hours at 25 C. The results are tabulated below.
in effectiveness with molecular weight, branching and structure, i.e., from primary to tertiary.
4. Example 4 Runs 1 2 3 Run Temp, C 25 25 10 Al/Ti ratio 3 5 Yield, ml 170 330 230 Solid polymer:
M.W.XIO- 17.8 14. 0 23.0
Vol. percent 74 9 5 ClO'lzEt] oil and Soluble wax, v percent ca. 25 91 77 C41 olefins, vol. percent ea. 1 0 18 These results show the unexpected effect of decreasing molecular weight with increasing Al/ Ti ratio. Decreasing the temperature decreased the average molecular weight and gave high selectively to low molecular weight olefins.
Example 5 A similar run is performed as in Example 3 but a temperature of C. and o-dichlorobenzene are used. Over 95% selectivity to oils is thus obtained. In general the more polar diiuents permit employment of higher temperatures Without producing solid polymers.
The products of this invention are useful as motor lube base stocks, olefinic synthetic intermediates, hydraulic transmission fluids, pour depressants, synthetic jet engine oils and bright stocks, among others. These products can also be hydrogenated without any diminution in viscosity index.
The advantages of this invention will be apparent to the skilled in the art. Useful oils are prepared in an ethcient and economic manner. A process of increased flexibility is provided.
It is to be understood that this invention is not limited to the specific examples which have been offered merely as illustrations and that modifications may be made without departing from the spirit of the invention.
What is claimed is:
1. In a method of preparing a hydrocarbon oil having a molecular weight in the range of 80 to 2000, said oil being suitable for lubricating purposes which comprises polymerizing an ethylene-containing gas in the presence of a catalyst consisting of a halide of a transition metal selected from the group consisting of titanium, zirconium, and vanadium and an aluminum alkyl compound having the formula AlR X n representing a number of at least 1. but less than 2 in the presence of a halogenated aromatic hydrocarbon diluent, at a pressure of 0-50 p.s.i.g., the improvement which comprises utilizing a minor amount of a C -C alkanol as a catalyst modifier, said alkanol being present in an amount such that the ratio of alkanol to the alkyl of the aluminum alkyl after reduction of the transition metal halide is not greater than 0.5 1.
2. The method of claim 1 in which the alkanol has from 1 to 4 carbon atoms.
Th6 Process of claim. 2 in which a maximum temperature of C. is employed.
4. The process of claim 3 in which the halogenated hydrocarbon diluent is monochlorobenzene.
5. The process of claim 4 in which the alkanol is tertiary butanol.
6. The process of claim 4 in which the alkanol is isopropanol.
7. The process of claim 3 in which the metal halide is Mme.
TiCl and the aluminum alkyl is aluminum ethyl dichloride.
8. The process of claim 3 in which the halogenated diluent is a dichlorobenzene.
9. The process of claim 4 in which the alkanol is methanol.
10. The process of claim 5 in which the metal halide is TiCl and the aluminum alkyl is aluminum ethyl dichloride.
11. The process of claim 10 wherein the ratio of alkanol to alkyl is in the range of 0.2/1 to 0.33/1.
References Cited in the file of this patent UNITED STATES PATENTS Boultbee Aug. 29, 1939 Bestian et al Oct. 6, 1959 Nowlin et al Jan. 24, 1961 White et a1 July 25, 1961 Boehm et al Dec. 31, 1963 FOREIGN PATENTS Great Britain Mar. 4, 1959 France Mar. 9, 19-59

Claims (1)

1. IN A METHOD OF PREPARING A HYDROCARBON OIL HAVING A MOLECULAR WEIGHT IN THE RANGE OF 80 TO 2000, SAID OIL BEING SUITABLE FOR LUBRICATING PURPOSES WHICH COMPRISES POLYMERIZING AN ETHYLENE-CONTAINING GAS IN THE PRESENCE OF A CATALYST CONSISTING OF A HALIDE OF A TRANSITION METAL SELECTED FROM THE GROUP CONSISTING OF TITANIUM, ZIRCONIUM, AND VANADIUM AND AN ALUMINUM ALKYL COMPOUND HAVING THE FORMULA AIRNX3-N, N REPRESENTING A NUMBER OF AT LEAST 1 BUT LESS THAN 2 IN THE PRESENCE OF A HALOGENATED AROMATIC HYDROCARBON DILUENT, AT A PRESSURE OF 0-50 P.S.I.G., THE IMPROVEMENT WHICH COMPRISES UTILIZING A MINOR AMOUNT OF A C1-C8 ALKANOL AS A CATALYST MODIFIER, SAID ALKANOL BEING PRESENT IN AN AMOUNT SUCH THAT THE RATIO OF ALKANOL TO THE ALKYL OF THE ALUMINUM ALKYL AFTER REDUCTION OF THE TRANSITION METAL HALIDE IS NOT GREATER THAN 0.5/1.
US55845A 1960-09-14 1960-09-14 Polymerized ethylene lubricating oils from alkanol modified catalysts Expired - Lifetime US3168588A (en)

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US55845A US3168588A (en) 1960-09-14 1960-09-14 Polymerized ethylene lubricating oils from alkanol modified catalysts
GB30054/61A GB920145A (en) 1960-09-14 1961-08-21 Polymerized ethylene lubricating oils from alkanol modified catalysts
US413347A US3474157A (en) 1960-09-14 1964-11-23 Polymerized ethylene pour point depressants from alkanol modified catalysts
US783699A US3662021A (en) 1960-09-14 1968-12-13 Process for preparing linear olefins
US05/882,946 US4396788A (en) 1960-09-14 1978-03-02 Preparation of linear olefin products
US06/179,655 US4409414A (en) 1960-09-14 1980-08-20 Preparation of linear olefin products
US06/330,596 US4442309A (en) 1960-09-14 1981-12-14 Preparation of linear olefin products
US06/454,379 US4486615A (en) 1960-09-14 1982-12-29 Preparation of linear olefin products

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US3316321A (en) * 1963-01-22 1967-04-25 Raffinage Cie Francaise Method of manufacturing alpha-olefins by oligomerization
US3413376A (en) * 1964-09-14 1968-11-26 Phillips Petroleum Co Catalysts and method for the preparation of liquid olefin polymers
US3457244A (en) * 1964-04-28 1969-07-22 Mitsubishi Petrochemical Co Process for preparing a polymer
US3474157A (en) * 1960-09-14 1969-10-21 Exxon Research Engineering Co Polymerized ethylene pour point depressants from alkanol modified catalysts
US3492245A (en) * 1966-03-28 1970-01-27 Goodyear Tire & Rubber Catalyst composition comprising an organoaluminum compound,a tungsten hexahalide and a compound of the formula roh
US3506573A (en) * 1968-05-29 1970-04-14 Mobil Oil Corp Greases containing a hydrogenated olefin polymer vehicle,organophilic clay thickener and calcium acetate dispersion
US3514401A (en) * 1963-09-26 1970-05-26 Mobil Oil Corp Greases containing hydrogenated olefin polymer vehicle and organophilic clay thickener
US3676521A (en) * 1970-10-05 1972-07-11 Sun Oil Co Synthetic lubricants from low molecular weight olefins
JPS4918186A (en) * 1972-04-17 1974-02-18
US3882046A (en) * 1973-01-03 1975-05-06 Anatoly Dmitrievich Pomogailo Catalyst for polymerization and copolymerization of olefines and a method for preparing same
US4031020A (en) * 1974-05-31 1977-06-21 Nippon Oil Company, Ltd. Central system fluid composition
US4396788A (en) * 1960-09-14 1983-08-02 Exxon Research And Engineering Co. Preparation of linear olefin products
US5116795A (en) * 1985-08-02 1992-05-26 Quantum Chemical Corporation Alpha olefin oligomerization catalyst
US5122581A (en) * 1985-08-02 1992-06-16 Quantum Chemical Corporation Polymerization method
WO1999047627A1 (en) * 1998-03-20 1999-09-23 Mobil Business Resources Corporation Synthesis of branched polyethylene fluids for use in lubricant compositions
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Cited By (19)

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US3474157A (en) * 1960-09-14 1969-10-21 Exxon Research Engineering Co Polymerized ethylene pour point depressants from alkanol modified catalysts
US4396788A (en) * 1960-09-14 1983-08-02 Exxon Research And Engineering Co. Preparation of linear olefin products
US3316321A (en) * 1963-01-22 1967-04-25 Raffinage Cie Francaise Method of manufacturing alpha-olefins by oligomerization
US3514401A (en) * 1963-09-26 1970-05-26 Mobil Oil Corp Greases containing hydrogenated olefin polymer vehicle and organophilic clay thickener
US3457244A (en) * 1964-04-28 1969-07-22 Mitsubishi Petrochemical Co Process for preparing a polymer
US3413376A (en) * 1964-09-14 1968-11-26 Phillips Petroleum Co Catalysts and method for the preparation of liquid olefin polymers
US3492245A (en) * 1966-03-28 1970-01-27 Goodyear Tire & Rubber Catalyst composition comprising an organoaluminum compound,a tungsten hexahalide and a compound of the formula roh
US3506573A (en) * 1968-05-29 1970-04-14 Mobil Oil Corp Greases containing a hydrogenated olefin polymer vehicle,organophilic clay thickener and calcium acetate dispersion
US3676521A (en) * 1970-10-05 1972-07-11 Sun Oil Co Synthetic lubricants from low molecular weight olefins
JPS4918186A (en) * 1972-04-17 1974-02-18
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US3882046A (en) * 1973-01-03 1975-05-06 Anatoly Dmitrievich Pomogailo Catalyst for polymerization and copolymerization of olefines and a method for preparing same
US4031020A (en) * 1974-05-31 1977-06-21 Nippon Oil Company, Ltd. Central system fluid composition
US5116795A (en) * 1985-08-02 1992-05-26 Quantum Chemical Corporation Alpha olefin oligomerization catalyst
US5122581A (en) * 1985-08-02 1992-06-16 Quantum Chemical Corporation Polymerization method
WO1999047627A1 (en) * 1998-03-20 1999-09-23 Mobil Business Resources Corporation Synthesis of branched polyethylene fluids for use in lubricant compositions
US6063973A (en) * 1998-03-20 2000-05-16 Mobil Oil Corporation Synthesis of branched polyethylene fluids for use in lubricant compositions
US6150576A (en) * 1998-03-20 2000-11-21 Mobil Oil Corporation Synthesis of branched polyethylene fluids for use in lubricant compositions
US20030116290A1 (en) * 2001-12-20 2003-06-26 3M Innovative Properties Company Continuous process for controlled evaporation of black liquor

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